Abstract

Organotypic, three dimensional (3D) cell culture models of epithelial tumour types such as prostate cancer recapitulate key aspects of the architecture and histology of solid cancers. Morphometric analysis of multicellular 3D organoids is particularly important when additional components such as the extracellular matrix and tumour microenvironment are included in the model. The complexity of such models has so far limited their successful implementation. There is a great need for automatic, accurate and robust image segmentation tools to facilitate the analysis of such biologically relevant 3D cell culture models. We present a segmentation method based on Markov random fields (MRFs) and illustrate our method using 3D stack image data from an organotypic 3D model of prostate cancer cells co-cultured with cancer-associated fibroblasts (CAFs). The 3D segmentation output suggests that these cell types are in physical contact with each other within the model, which has important implications for tumour biology. Segmentation performance is quantified using ground truth labels and we show how each step of our method increases segmentation accuracy. We provide the ground truth labels along with the image data and code. Using independent image data we show that our segmentation method is also more generally applicable to other types of cellular microscopy and not only limited to fluorescence microscopy.

Highlights

  • Cellular processes naturally occur in three dimensions (3D) and cells are typically embedded in extracellular matrix, which is a key component of the cellular microenvironment

  • We present a series of results in order to discuss the benefits of our Markov random fields (MRFs) based method for our complex biological application, in particular, multichannel 3D image data with large distances between images in the stack

  • We show the utility of the local entropy filter and that our MRF based approach obtains the most accurate segmentation results

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Summary

Introduction

Cellular processes naturally occur in three dimensions (3D) and cells are typically embedded in extracellular matrix, which is a key component of the cellular microenvironment. Physiologically relevant cell culture models are increasingly designed in 3D formats embedded. VTT provided support in the form of salaries for authors SR, MÅ, and MN, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. MT has worked as an external researcher affiliated to VTT through the research group (led by MN). The specific roles of these authors are articulated in the author contributions section

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